
Text extracted from the exhibit documents filed with the FCC. Open a document above to read the original.
AiDEX TM Continuous Glucose Monitoring System User Guide 0344 MicroTech Medical (Hangzhou) Co., Ltd. Index Important safety information 1 Indications for use .................................................... 2 Patients .................................................................... 2 Contraindications ...................................................... 3 Precautions .............................................................. 3 Product components 6 Component description ...........................................10 Accessories.............................................................15 Using a New Glucose Sensor 17 Applying a sensor .................................................. 17 Setting the Personal Diabetes Assistant (PDA) for the first time ...................................................... 22 Sensor start-up ...................................................... 24 Sensor calibration .................................................. 28 Removing a sensor 31 PDA settings 33 Target glucose range ............................................ 33 Date and time settings .......................................... 35 Using the PDA 36 Pairing with a new transmitter .............................. 36 PDA cautions .................................................... 40 Charing the Personal Diabetes Assistant (PDA) .. 41 Caring for your Continuous Glucose Monitoring System (CGMS) .................................. 42 Electromagnetic compatibility 50 Appendix 59 1 Important safety information Indications for use The Continuous Glucose Monitoring System (CGMS) is indicated for continuous or regular monitoring of glucose levels in subcutaneous tissue, and is used for daily detection and self-management of blood glucose levels in people 2 years and older. It is intended for use by patients at home and in healthcare facilities. Interpretation of the CGMS results should be based on the glucose trends and several sequential readings over time . The CGMS also aids in the detection of episodes of hyperglycemia and hypoglycemia, and facilitating therapy adjustments . The System is designed to replace fingerstick blood glucose (BG) testing. 2 Patients This Continuous Glucose Monitoring System is suit- able for patients with diabetes requiring regular blood glucose monitoring. Contraindications Patients who: 1. Suffer from alcoholism, drug abuse, severe mental disorders (such as depression, schizophrenia). 2. Are unconscious. 3. Are unable to understand or master the usage of the device. 4. Have severe hearing or vision impairment. 5. User below the age of 2 or are not capable of admin- istering diabetes therapy themselves or who always 3 need to use Continuous Glucose Monitor under strict supervision of parents or qualified healthcare professionals. Precautions • CGMS readings should only be used as a reference for the supplemental monitoring of diabetes mellitus and should not be used as a basis for clinical diagno- sis. • The CGMS should be completely removed before Magnetic Resonance Imaging (MRI). • The CGMS contains many small parts that can be dangerous if swallowed. • During rapid changes in blood glucose (more than 0. 1mmol/L per minute), glucose levels measured in interstitial fluid by the CGMS may not be the same as blood glucose levels. When blood glucose lev- els drop rapidly, the sensor may produce a higher reading than the blood glucose level; Conversely, 4 when blood glucose levels rise rapidly, the sensor may produce a lower reading than the blood glucose level. When experiencing symptoms of hypoglycemic or hyperglycemic, the sensor readings are checked by using a blood glucose meter for a fingertip blood glucose test. • Severe dehydration or excessive loss of water may result in inaccurate results. When you suspect you are dehydrated, consult a heathcare professional immediately. • If you think the CGMS sensor reading is inaccurate or inconsistent, use a blood glucose meter to test your blood glucose level or calibrate the glucose sensor. If the problem persists, remove and replace the sensor. • While extensive user testing was done on AiDEX TM CGMS in Type I and Type II diabetic patients, the study groups did not include women with gestational diabetes. • The performance of the CGMS has not been eval- uated when used with another implantable medical device, such as a pacemaker. 5 • Only MicroTech Medical consumables should be used with the CGMS. • If the product is not working properly or has been damaged, stop using the product. • When used in a medical facility, the operator should wear gloves while using. • The CGMS can not be used in oxygen rich enviro- ment. • Operator or the responsible organization shall read this instructions for use as the training or the knowledge required for using this equipment. • Any serious injury or death that has occurred in relation to the device should be reported to the man- ufacturer and the competent authority of the Member State in which the user and/or patient is established. 6 Product components Name: AiDEX™ continuous glucose monitoring sys- tem System configuration: This product includes a Per- sonal Diabetes Assistant, a Transmitter and a Glucose Sensor. Personal Diabetes Assistant will be referred as PDA in the text below. System Sensor Transmitter PDA G7 G7-S01 G7-T01 G7-P02、 MTM-2 G7-A G7-S01A G7-T01A G7-B G7-S01B G7-T01B 7 The PDA & Transmitter system consists of the fol- lowing components: • Personal Diabetes Assistant (Li-ion battery included) •Transmitter 8 Warning :No modification of this equipment is allowed. Unauthorized modification of the equipment may cause the product to malfunction and become unusable.Replacement of a component could result in an unacceptable risk. Warning :Remove the battery if not used for a long time ! If the PDA battery charger does not work, do not try to repair it. Please contact your local supplier for a replacement. Note:The device is intended to be transported and stored in waterp…
Text truncated - open the document above for the full version.
MicroTech Medical (Hangzhou) Co., Ltd. No. 108 Liuze St., Cangqian, Yuhang District, Hangzhou, 311121 Zhejiang, P.R. China DATE : 06/06/2023 MicroTech Medical (Hangzhou) Co., Ltd. No. 108 Liuze St., Cangqian, Yuhang District, Hangzhou, 311121 Zhejiang, P.R. China Attn: Director of Certification Authority to Act as Agent On our behalf, I appoint below company and person: Name Damon Hu Position Manager Company Name Dongguan Dongdian Testing Service Co.,Ltd. Address 17, Zongbu Road 2, Songshan Lake Sci&Tech, Industry Park, Dongguan City, Guangdong Province, China, 523808 Tel / Fax Tel: +86-0769-38826678-850 E-Mail [email protected] to act as our agent in the preparation of this application for equipment certification. I certify that submitted documents properly describe the device or system for which equipment certification is sought. I also certify that each unit manufactured, imported or marketed, as defined in the Federal Communications Commission’s regulations will have affixed to it a label identical to that submitted for approval with this application. Applicant name MicroTech Medical (Hangzhou) Co., Ltd. Address No. 108 Liuze St., Cangqian, Yuhang District, Hangzhou, 311121 Zhejiang, P.R. China Yours sincerely, Signatory Name Leo wang Position Registration Specialist Company Name MicroTech Medical (Hangzhou) Co., Ltd. Address No. 108 Liuze St., Cangqian, Yuhang District, Hangzhou, 311121 Zhejiang, P.R. China Tel +86 18621889766 E-Mail [email protected] MicroTech Medical (Hangzhou) Co., Ltd. No. 108 Liuze St., Cangqian, Yuhang District, Hangzhou, 311121 Zhejiang, P.R. China
C5266091_X24_Ed.2 1/1 “Attestation Statements” TO: Office of Engineering Technology Federal Communications Commission 7435 Oakland Mills Road Columbia, MD 21046 The Commission adopted rules that prohibit equipment authorization for “covered” telecommunications equipment and video surveillance equipment produced by entities identified on the Commission’s Covered List 1 , which is periodically updated. See the Covered List for more details. This Attestation Statement is to confirm that we follow the Section 2.911(d)(5)(i)-(ii) Applicant Company name: MicroTech Medical (Hangzhou) Co., Ltd. Grantee code: 2ATOV FCC ID: 2ATOV-T-G7 Contact Name: Leo wang Address: No. 108 Liuze St., Cangqian, Yuhang District, Hangzhou, 311121 Zhejiang, P.R. China Telephone No: +86 18621889766 Email: [email protected] i. MicroTech Medical (Hangzhou) Co., Ltd. (“the applicant”) certifies that the equipment for which authorization is sought is not “covered” equipment prohibited from receiving an equipment authorization pursuant to section 2.903 of the FCC rules. The applicant must sign this certification. ii. MicroTech Medical (Hangzhou) Co., Ltd. (“the applicant”) certifies that, as of the date of the filing of the application, the applicant is not (as a specifically named entity or any of its subsidiaries or affiliates) identified on the Covered List as an entity producing “covered” equipment. The applicant must sign this certification. MicroTech Medical (Hangzhou) Co., Ltd. (“the applicant”) certifies that, as of the date of the filing of the application, the applicant is not identified on the Covered List as an entity producing “covered” equipment. Date: 2023/06/06 Applicant’s Name: Leo wang Title: Registration Specialist Signature 1 The Commission’s Covered List is published by the Public Safety and Homeland Security Bureau and posted on the Commission’s website. This Covered List, which is periodically updated, identifies particular equipment, produced by particular entities, that constitutes “covered” equipment. https://www.fcc.gov/supplychain/coveredlist
1/1 Declaration of difference Date: 2023/06/06 To Whom It May Concern: The Product: Transmitter Model No.: G7-T01, G7-T01A, G7-T01B All model circuits share the same electrical, mechanical and physical structure, with the only difference is the working hours. The duration is 14 days for G7- T01, 10 days for G7-T01A, and 7 days for G7-T01B. There is no influence on the test results. Yours sincerely, Signatory Name Leo wang Position Registration Specialist Company Name MicroTech Medical (Hangzhou) Co., Ltd. Address No. 108 Liuze St., Cangqian, Yuhang District, Hangzhou, 311121 Zhejiang, P.R. China Tel +86 18621889766 E-Mail [email protected]
C5266091_X8_Ed.1 1/1 Letter of Authorization MicroTech Medical (Hangzhou) Co., Ltd. Company: MicroTech Medical (Hangzhou) Co., Ltd. Address: No. 108 Liuze St., Cangqian, Yuhang District, Hangzhou, 311121 Zhejiang, P.R. China Product Name: Transmitter Model Number: G7-T01, G7-T01A, G7-T01B FCC Identifier: 2ATOV-T-G7 We authorize LGAI Technological Center S.A., Ronda de la Font del Carme, s/n, 08193 Bellaterra, Spain, to act on our behalf on all matters concerning the above named equipment. Any individual within LGAI Technological Center S.A. is authorized to act on our behalf and take action on the application. We declare that authorize LGAI Technological Center S.A., Ronda de la Font del Carme, s/n, 08193 Bellaterra, Spain, is allowed to forward all information related to the approval project to the Federal Communication Commission and to discuss any issues concerning the approval application. Any and all acts carried out by LGAI Technological Center S.A. on our behalf shall have the same effect as acts of our own. Name: Leo wang Date: 2023/06/06 Title: Registration Specialist Signature of applicant:
C5266091_X10_Ed.1 1/1 MicroTech Medical (Hangzhou) Co., Ltd. Office of Engineering Technology Federal Communications Commission 7435 Oakland Mills Road Columbia, MD 21046 Date: 2023/06/06 Subject: Request for Confidentiality FCC ID: 2ATOV-T-G7 To Whom It May Concern, Pursuant to the provisions of Sections 0.457 and 0.459 of Commission's rules (47CFR0.457, 0.459), we are requesting the Commission to withhold the following attachment(s) as confidential document from public disclosure. Exhibits Long-Term Confidentiality Short-Term Confidentiality ID Label/Location No No Attestation Statement No No External Photos No Block Diagram Schematics Test Report No No Test Setup Photos No User’s Manual Internal Photos Parts List / Tune Up RF Exposure Info Operational Description Cover Letter(s) No No SDR Software / Security Info No In case of short-term Confidentiality, the applicant requests the exhibits selected above are withheld from public view for a period of _180_ days from the date of the Grant of Equipment Authorization and prior to marketing. Above mentioned document contains detailed system and equipment description are considered as proprietary information in operation of the equipment. The public disclosure of above documents might be harmful to our company and would give competitor an unfair advantage in the market. It is our understanding that all measurement test reports, FCC ID label format and correspondent during certification review process cannot be granted as confidential documents and those information will be available for public review once the grant of equipment authorization is issued. Sincerely, Signature: C5266091_X10_Ed.1 1/1 Name: Leo wang Title: Registration Specialist
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Dongguan Dongdian Testing Service Co., Ltd. Report No.:DDT-R22081519-2E04 Page 1 of 6 RF EXPOSURE REPORT FOR Issued By: Dongguan Dongdian Testing Service Co., Ltd. Add.: No. 17, Zongbu Road 2, Songshan Lake Sci&Tech, Industry Park, Dongguan City, Guangdong Province, China, 523808 Tel.: +86-0769-38826678, E-mail: [email protected], http://www.dgddt.com Applicant : MicroTech Medical (Hangzhou) Co., Ltd. Address : No.108 Liuze St., Cangqian, Yuhang District, Hangzhou 311121 Zhejiang P.R.China Equipment under Test : Transmitter Model No. : G7-T01, G7-T01A, G7-T01B Trade Mark : FCC ID : 2ATOV-T-G7 Manufacturer : MicroTech Medical (Hangzhou) Co., Ltd. Address : No.108 Liuze St., Cangqian, Yuhang District, Hangzhou 311121 Zhejiang P.R.China Report No.: DDT-R22081519-2E04 Issued Date: Sep. 15, 2022 Dongguan Dongdian Testing Service Co., Ltd. Report No.:DDT-R22081519-2E04 Page 2 of 6 Table of Contents Test report declares........................................................................................................3 1. General Information ....................................................................................................... 5 1.1. Description of equipment ............................................................................................... 5 1.2. Assess laboratory ........................................................................................................... 5 2. RF Exposure evaluation for FCC ................................................................................... 5 Dongguan Dongdian Testing Service Co., Ltd. Report No.:DDT-R22081519-2E04 Page 3 of 6 Test Report Declare Standard Used: KDB447498 D01 General RF Exposure Guidance v06 We Declare: The equipment described above is assessed by Dongguan Dongdian Testing Service Co., Ltd. and in the configuration assessed the equipment complied with the standards specified above. The assessed results are contained in this report and Dongguan Dongdian Testing Service Co., Ltd. is assumed of full responsibility for the accuracy and completeness of these assess. After evaluation, our opinion is that the equipment In Accordance with above standard. Report No: DDT-R22081519-2E04 Date of Receipt: Aug. 26, 2022 Date of Test: Aug. 26, 2022 ~ Sep. 15, 2022 Prepared By: Approved By: _____________________ _____________________ Sanvin Zheng/Engineer Damon Hu/EMC Manager Note: This report applies to above tested sample only. This report shall not be reproduced in parts without written approval of Dongguan Dongdian Testing Service Co., Ltd. Applicant : MicroTech Medical (Hangzhou) Co., Ltd. Address : No.108 Liuze St., Cangqian, Yuhang District, Hangzhou 311121 Zhejiang P.R.China Equipment under Test : Transmitter Model No. : G7-T01, G7-T01A, G7-T01B Trade mark : Manufacturer : MicroTech Medical (Hangzhou) Co., Ltd. Address : No.108 Liuze St., Cangqian, Yuhang District, Hangzhou 311121 Zhejiang P.R.China E S T T I N N A I G D S G E N R O V D I C E N A C U O G . , G L N T O D D . Dongguan Dongdian Testing Service Co., Ltd. Report No.:DDT-R22081519-2E04 Page 4 of 6 Revision History Rev. Revisions Issue Date Revised By --- Initial issue Sep. 15, 2022 Dongguan Dongdian Testing Service Co., Ltd. Report No.:DDT-R22081519-2E04 Page 5 of 6 1. General Information 1.1. Description of equipment 1.2. Assess laboratory Dongguan Dongdian Testing Service Co., Ltd. Add.: No. 17, Zongbu Road 2, Songshan Lake Sci&Tech, Industry Park, Dongguan City, Guangdong Province, China, 523808. Tel.: +86-0769-38826678, http://www.dgddt.com, Email: [email protected]. CNAS Accreditation No. L6451; A2LA Accreditation Number: 3870.01 FCC Designation Number: CN1182, Test Firm Registration Number: 540522 Innovation, Science and Economic Development Canada Site Registration Number: 10288A Conformity Assessment Body identifier: CN0048 VCCI facility registration number: C-20087, T-20088, R-20123, R-20155, G-20118 2. RF Exposure evaluation for FCC According to 447498 D01 General RF Exposure Guidance v06 The 1-g and 10-g SAR test exclusion thresholds for 100 MHz to 6 GHz at test separation distances ≤ 50 mm are determined by: [(max. power of channel, including tune-up tolerance, mW)/(min. test separation distance, mm)] ·[√f(GHz)] ≤ 3.0 for 1-g SAR and ≤ 7.5 for 10-g extremity SAR, where: f(GHz) is the RF channel transmit frequency in GHz Power and distance are rounded to the nearest mW and mm before calculation The result is rounded to one decimal place for comparison EUT* Name : Transmitter Model Number : G7-T01, G7-T01A, G7-T01B Model difference : All model circuits share the same electrical, mechanical and physical structure, with the only difference is the working hours. The duration is 14 days for G7-T01, 10 days for G7-T01A, and 7 days for G7-T01B. Therefore, the test model is G7-T01. EUT function description : Please reference user manual of this device Power Supply : DC 3V button cell built-in battery Radio Specification : Bluetooth V5.0 Operation Frequency : 2402 MHz - 2480 MHz Modulation : GFSK Data Rate : 1 Mbps Antenna Gain : FPC antenna, maximum PK gain: -2.41 dBi Sample Number : S22081519-03 for conductive S22081519-04 for radiation Dongguan Dongdian Testing Service Co., Ltd. Report No.:DDT-R22081519-2E04 Page 6 of 6 Manufacturing Tolerance BLE GFSK (Peak) 1M Channel Channel 0 Channel 39 Channel 78 Target (dBm) -0.42 -0.63 -0.50 Tolerance ±(dB) 1 1 1 Estimtion Result Worse case is as below: [2402 MHz, 0.58 dBm, (1.14 mW) output power] (1.14/5) ·[√2.402(GHz)] = 0.35 < 3.0 for 1-g SAR Then SAR evaluation is not required. END OF REPORT
项目: Aidex 撰写: Zhang_shi bin 文件名: 微泰泵- Aidex-规格书 日期: 2022.09.21 版本 V2.2 审核: Lipeng 模具品 CONFIDENTIAL Brotone.com Page - 1 - 坤鹏通达科技有限公司 Broadband Electronics Technology Co.,Ltd 样品规格书 ANTENNA APPROVAL SHEET 客户:微泰泵 项目:Aidex (优金手指) 项目频段 WIFI2.4G/BT 制表日期 2022.09.21 射频工程师/RF 孔祥华 结构工程师 /MD 张海东 客户硬件 客户项目 客户结构/MD 客户品质 地址 深圳南山区高新科技园北区第五工业区办公大楼五楼 电话 13902948715 网站 www.kpantenna.com 公司邮箱 [email protected] 联系人 李鹏 项目: Aidex 撰写: Zhang_shi bin 文件名: 微泰泵- Aidex-规格书 日期: 2022.09.21 版本 V2.2 审核: Lipeng 模具品 CONFIDENTIAL Brotone.com Page - 2 - 项目: Aidex 撰写: Zhang_shi bin 文件名: 微泰泵- Aidex-规格书 日期: 2022.09.21 版本 V2.2 审核: Lipeng 模具品 CONFIDENTIAL Brotone.com Page - 3 - 1. Project information and Electrical Specification Those specifications were specially defined for 微泰泵Aidex, WIFI2.4G/ BT, and all characteristics were measured umnder the model 's handset testing jig . 1-1 Antenna picture 1-2 Frequency Band: Frequency Band MHz WIFI2.4G 2400-2500(MHz) 1-3 Impedance matching 天线原匹配无更改 2. VSWR Measuring Method: 1.A 50 2cocaxial cable is connected to the antenma. Then this cable is commected to a network amalyzer to mecasure the VSWR, 2. Keeping this jig n1way from metal at least 20cm. 项目: Aidex 撰写: Zhang_shi bin 文件名: 微泰泵- Aidex-规格书 日期: 2022.09.21 版本 V2.2 审核: Lipeng 模具品 CONFIDENTIAL Brotone.com Page - 4 - VSWR parameter values VSWR parameter values 频率(MHz) 2400 2450 2500 驻波 2.5 2.1 1.9 Smith R+jX 项目: Aidex 撰写: Zhang_shi bin 文件名: 微泰泵- Aidex-规格书 日期: 2022.09.21 版本 V2.2 审核: Lipeng 模具品 CONFIDENTIAL Brotone.com Page - 5 - Smith G+jB 项目: Aidex 撰写: Zhang_shi bin 文件名: 微泰泵- Aidex-规格书 日期: 2022.09.21 版本 V2.2 审核: Lipeng 模具品 CONFIDENTIAL Brotone.com Page - 6 - 3. Efficiency and Gain*measuring and test instruments: 微波暗室,Agilent 网络分析仪,Agilent 频谱分析仪,8960 综合测试仪,标准天线 *test method: equipment以H面放于转台中心位置固定,与喇叭天线中心位置在同一个水平线上。. Efficiency/Gain- WIFI2.4G 项目: Aidex 撰写: Zhang_shi bin 文件名: 微泰泵- Aidex-规格书 日期: 2022.09.21 版本 V2.2 审核: Lipeng 模具品 CONFIDENTIAL Brotone.com Page - 7 - 4.天线位置图 天线安装位置请参考上图 包装方式 物料类别 包装方式 举例图示 (unit: dBi) (unit: dBi) (unit: dBi) (unit: dBi) (unit: dBi) (unit: dBi) (unit: dBi) (unit: dBi) (unit: dBi) 项目: Aidex 撰写: Zhang_shi bin 文件名: 微泰泵- Aidex-规格书 日期: 2022.09.21 版本 V2.2 审核: Lipeng 模具品 CONFIDENTIAL Brotone.com Page - 8 - FPC 1、密封PE袋包装, 200PCS/小袋 2、20小袋/大袋 3、外面以纸箱打包出 货.(根据出货数量, 纸箱大小会有不同) 备注:请将本产品储存在低温、低湿(温度18-28°C,湿度35%-75%RH)无腐 蚀性气体的环境下,建议开包后一周内使用完,使用中请尽量不要让产品3M 胶有指纹,以免影响粘着力。 OQC检验测试报告 订单号 客户料号 检测 项目 抽样计划 AQL AC RE 判定 客户型号 Aidex 外观 CR 0.15 0.15 0 1 数量 出货数量 Pcs MAJ 0.4 0.4 2 3 合格 抽样数量: Pcs MIN 0.65 0.65 3 4 1.开路 NIL 10.凹坑/压伤 NIL 19.离型纸未切断 NIL 2.短路 NIL 11.电镀粗脏、金面水印 NIL 20.金面氧化 NIL 3.线路起翘 NIL 12.金面针孔、缺口 NIL 21.冲偏/露铜 NIL 4.线路损坏 NIL 13.胶层气泡 NIL 22.未冲断 NIL 5.擦/刮花 NIL 14.油墨颜色 NIL 23.掉金/甩金 NIL 6.露铜/镍 NIL 15.字符不清 NIL 24.弯曲/变形 NIL 7.掉油 NIL 16.垃圾/异物 NIL 25.外形缺口 NIL 8.氧化/变色 NIL 17溢胶/流胶 NIL 26.堆胶/缺胶 NIL 9.表面脏污 NIL 18.皱褶 NIL 27.补强不良 NIL 判定: √合格 □不合格 □特采出货 项目: Aidex 撰写: Zhang_shi bin 文件名: 微泰泵- Aidex-规格书 日期: 2022.09.21 版本 V2.2 审核: Lipeng 模具品 CONFIDENTIAL Brotone.com Page - 9 - 备注:请将本产品储存在低温、低湿(温度18-28°C,湿度35%-75%RH)无腐蚀性气体的环境下,建议开包后一周 内使用完。 可靠性测试 项目名称 要 求 实 测 结果 热冲击实验 288°C*10S'*3次 288°C*10S'*3次无分层、起泡 ok 抗剥离实验 ≥1.0㎏f/c㎡ 1.112㎏f/c㎡ ok 油墨拉力测试 3M600胶带垂直拉起 无掉油墨现象 ok 生产及检测设备清单 生产设备 检测设备1 检测设备2 蚀刻外形机 二次元摄影机 千分尺 检验员: 审核: 盐雾检测报告 产品型号 Aidex 测试数量 5PCS 测试标准 GB2423.17 货品素材 FPC 测试项目 要求标准 实际数值 判定 测试项目 要求标准 实际 数值 判定 测试仪器规 格 KD-60 KD-60 OK 测试时间 24H 24H OK 盐雾测试类 型 NSS中性 NSS中性 OK 盐雾箱温度 35°C 35°C OK 盐水PH值 6.5-7.2 6.8 OK 盐雾沉降量 (H.80C) 1-2ml 1.8ml OK 喷雾方式 连续喷雾 连续喷雾 OK 货品材质 FPC FPC OK 盐水成份 5%/NaCL 5%/NaCL OK 压缩空气节 压力 1±0.1KG/CM2 1 OK 饱和温度 47°C 47°C OK 试样放置角 度 90° 90° OK 项目: Aidex 撰写: Zhang_shi bin 文件名: 微泰泵- Aidex-规格书 日期: 2022.09.21 版本 V2.2 审核: Lipeng 模具品 CONFIDENTIAL Brotone.com Page - 10 - 测试观察时 间 观察现象 4H 无异常 12H 无异常 24H 无异常 48H 无异常 判定标准:依国标5944-86评级方法判定,9级以上为合格 最终判定结果 合格√ 不合格 测试人员 何本源 审核 王爱兵 审批 备注:常用的盐雾试验方法有:NSS中惦盐雾试验,AASS乙酸盐雾试验,CASS铜乙酸加速试验.
Dongguan Dongdian Testing Service Co., Ltd. Report No.: DDT-R22081519-2E02 Page 1 of 55 FCC CERTIFICATION TEST REPORT FOR Issued By: Dongguan Dongdian Testing Service Co., Ltd. Add.: No. 17, Zongbu Road 2, Songshan Lake Sci&Tech, Industry Park, Dongguan City, Guangdong Province, China, 523808 Tel.: +86-0769-38826678, E-mail: [email protected], http://www.dgddt.com Applicant : MicroTech Medical (Hangzhou) Co., Ltd. Address : No.108 Liuze St., Cangqian, Yuhang District, Hangzhou 311121 Zhejiang P.R.China Equipment under Test : Transmitter Model No. : G7-T01, G7-T01A, G7-T01B Trade Mark : FCC ID : 2ATOV-T-G7 Manufacturer : MicroTech Medical (Hangzhou) Co., Ltd. Address : No.108 Liuze St., Cangqian, Yuhang District, Hangzhou 311121 Zhejiang P.R.China Report No.: DDT-R22081519-2E02 Issued Date: Sep. 15, 2022 Dongguan Dongdian Testing Service Co., Ltd. Report No.: DDT-R22081519-2E02 Page 2 of 55 Table of Contents Test report declares.......................................................................................................4 1. Summary of Test Results ............................................................................................... 6 2. General Test Information ............................................................................................... 7 2.1. Description of EUT ......................................................................................................... 7 2.2. Accessories of EUT ........................................................................................................ 8 2.3. Assistant equipment used for test .................................................................................. 8 2.4. Block diagram of EUT configuration for test .................................................................. 8 2.5. Test environment conditions .......................................................................................... 8 2.6. Deviations of test standard............................................................................................. 9 2.7. Test laboratory ............................................................................................................... 9 2.8. Measurement uncertainty ............................................................................................... 9 3. Equipment Used During Test ....................................................................................... 10 4. 6 dB Bandwidth and 99% Bandwidth ........................................................................... 11 4.1. Block diagram of test setup .......................................................................................... 11 4.2. Limits ............................................................................................................................ 11 4.3. Test procedure ............................................................................................................. 11 4.4. Test result ..................................................................................................................... 12 4.5. Original test data .......................................................................................................... 12 5. Maximum Peak Output Power ..................................................................................... 15 5.1. Block diagram of test setup .......................................................................................... 15 5.2. Limits ............................................................................................................................ 15 5.3. Test procedure ............................................................................................................. 15 5.4. Test result ..................................................................................................................... 15 5.5. Original test data .......................................................................................................... 16 6. Power Spectral Density ................................................................................................ 17 6.1. Block diagram of test setup .......................................................................................... 17 6.2. Limits ............................................................................................................................ 17 6.3. Test procedure ............................................................................................................. 17 6.4. Test result ..................................................................................................................... 17 6.5. Original test data .......................................................................................................... 18 7. Band Edge Compliance (Conducted Method) ............................................................. 19 7.1. Block diagram of test setup .......................................................................................... 19 7.2. Limits ............................................................................................................................ 19 7.3. Test procedure ............................................................................................................. 19 7.4. Test result ..................................................................................................................... 19 7.5. Original test data .......................................................................................................... 20 8. Radiated Emission ....................................................................................................... 21 Dongguan Dongdian Testing Service Co., Ltd. Report No.: DDT-R22081519-2E02 Page 3 of 55 8.1. Block diagram of test setup .......................................................................................... 21 8.2. Limit ........................................................…
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Dongguan Dongdian Testing Service Co., Ltd. Report No.: DDT-R22081519-2E02 Page 53 of 55 13. Test Setup Photograph Dongguan Dongdian Testing Service Co., Ltd. Report No.: DDT-R22081519-2E02 Page 54 of 55
Dongguan · China
| # | Rule Parts | Frequency Range | Power Output |
|---|---|---|---|
| 1 | 15C | 2.40 GHz - 2.48 GHz | 900.00 µW |

Blood glucose meter
Equipment Class
DTS - Digital Transmission System
Personal Diabetes Assistant
Equipment Class
DTS - Digital Transmission System